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KRAS抑制剂:耐药驱动因素与联合策略

KRAS inhibitors: resistance drivers and combinatorial strategies.

作者信息

Isermann Tamara, Sers Christine, Der Channing J, Papke Bjoern

机构信息

Charité - Universitätsmedizin Berlin, Institute of Pathology, Berlin, Germany; German Cancer Consortium (DKTK), Partner Site Berlin, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Charité - Universitätsmedizin Berlin, Institute of Pathology, Berlin, Germany; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; Department of Pharmacology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

出版信息

Trends Cancer. 2025 Feb;11(2):91-116. doi: 10.1016/j.trecan.2024.11.009. Epub 2024 Dec 27.

Abstract

In 1982, the RAS genes HRAS and KRAS were discovered as the first human cancer genes, with KRAS later identified as one of the most frequently mutated oncogenes. Yet, it took nearly 40 years to develop clinically effective inhibitors for RAS-mutant cancers. The discovery in 2013 by Shokat and colleagues of a druggable pocket in KRAS paved the way to FDA approval of the first covalently binding KRAS inhibitors, sotorasib and adagrasib, in 2021 and 2022, respectively. However, rather than marking the end of a successful assault on the Mount Everest of cancer research, this landmark only revealed new challenges in RAS drug discovery. In this review, we highlight the progress on defining resistance mechanisms and developing combination treatment strategies to improve patient responses to KRAS therapies.

摘要

1982年,RAS基因HRAS和KRAS作为首批人类癌症基因被发现,KRAS后来被确定为最常发生突变的致癌基因之一。然而,开发针对RAS突变癌症的临床有效抑制剂却花费了近40年时间。2013年,肖卡特及其同事发现KRAS中有一个可成药口袋,为2021年和2022年分别获得美国食品药品监督管理局(FDA)批准的首批共价结合KRAS抑制剂索托拉西布和阿达格拉西布铺平了道路。然而,这一里程碑并非标志着对癌症研究“珠穆朗玛峰”的成功攻克的结束,而是在RAS药物研发中揭示了新的挑战。在本综述中,我们重点介绍了在确定耐药机制和制定联合治疗策略以改善患者对KRAS疗法的反应方面所取得的进展。

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